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173774-48-6

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173774-48-6 Usage

Description

(R)-1-N-BOC-4-N-BOC-PIPERAZINE-2-CARBOXYLIC ACID is a chemical compound that belongs to the class of piperazine carboxylic acids. It is a derivative of piperazine and is widely recognized for its role as a building block in the synthesis of various pharmaceutical compounds. (R)-1-N-BOC-4-N-BOC-PIPERAZINE-2-CARBOXYLIC ACID is characterized by the presence of BOC (tert-butoxycarbonyl) protecting groups on both nitrogen atoms, which are crucial for controlling the reactivity of the compound during chemical reactions. As a key intermediate, (R)-1-N-BOC-4-N-BOC-PIPERAZINE-2-CARBOXYLIC ACID is instrumental in the development of drugs for treating a range of disorders and diseases, making it an essential component in the pharmaceutical industry.

Uses

Used in Pharmaceutical Industry:
(R)-1-N-BOC-4-N-BOC-PIPERAZINE-2-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceutical compounds for the treatment of different disorders and diseases. Its presence of BOC protecting groups on nitrogen atoms allows for controlled reactivity during chemical reactions, facilitating the development of therapeutic agents with desired properties.
Used in Drug Synthesis:
(R)-1-N-BOC-4-N-BOC-PIPERAZINE-2-CARBOXYLIC ACID is utilized as a building block in the synthesis of drugs, contributing to the creation of novel therapeutic agents with improved efficacy and safety profiles. The BOC protecting groups on the nitrogen atoms enable selective reactions and functional group manipulations, allowing for the synthesis of complex drug molecules with specific pharmacological properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (R)-1-N-BOC-4-N-BOC-PIPERAZINE-2-CARBOXYLIC ACID serves as a valuable compound for the exploration of new drug candidates. Its unique structure and reactivity make it an attractive starting material for the design and synthesis of potential therapeutic agents, enabling researchers to investigate its potential in treating various medical conditions.
Overall, (R)-1-N-BOC-4-N-BOC-PIPERAZINE-2-CARBOXYLIC ACID is a versatile and essential compound in the pharmaceutical industry, playing a crucial role in the development of new drugs and therapeutic agents for the treatment of various disorders and diseases. Its unique properties and reactivity make it a valuable asset in drug synthesis, medicinal chemistry research, and the advancement of pharmaceutical science.

Check Digit Verification of cas no

The CAS Registry Mumber 173774-48-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,7,7 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 173774-48:
(8*1)+(7*7)+(6*3)+(5*7)+(4*7)+(3*4)+(2*4)+(1*8)=166
166 % 10 = 6
So 173774-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H26N2O6/c1-14(2,3)22-12(20)16-7-8-17(10(9-16)11(18)19)13(21)23-15(4,5)6/h10H,7-9H2,1-6H3,(H,18,19)/t10-/m1/s1

173774-48-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-1,4-Bis(tert-butoxycarbonyl)piperazine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names (2R)-1,4-bis[(2-methylpropan-2-yl)oxycarbonyl]piperazine-2-carboxylic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:173774-48-6 SDS

173774-48-6Downstream Products

173774-48-6Relevant articles and documents

Bis(vinylsulfonyl)piperazines as efficient linkers for highly homogeneous antibody-drug conjugates

Huang, Rong,Sheng, Yao,Wei, Ding,Yu, Jianghui,Chen, Hongli,Jiang, Biao

, (2020)

Disulfide re-bridging strategy has demonstrated significant advantages in the construction of homogeneous antibody drug conjugates (ADCs). However, a major issue that disulfide scrambling at the hinge region of antibody leads to the formation of “half-antibody” has appeared for many re-bridging linkers. We present bis(vinylsulfonyl)piperazines (BVP) as efficient linkers to selectively re-bridge disulfides at the antigen-binding fragment (Fab) regions and produce highly homogeneous conjugates with a loading of two drugs without disulfide scrambling. We also found that optically active (S)-configuration linkers led to more sufficient conjugation compared with (R)-configuration. The BVP-linked ADCs demonstrated superior efficacy and antigen-selectivity in vitro cytotoxicity.

HETEROCYCLIC COMPOUNDS FOR THE TREATMENT OF ABNORMAL CELLULAR PROLIFERATION

-

Page/Page column 151, (2019/07/20)

This invention is in the area of heterocyclic-based compounds for the treatment of disorders involving abnormal cellular proliferation, including but not limited to tumors and cancers.

Human Adam-10 Inhibitors

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Page/Page column 20-21, (2011/01/12)

Magnesium salts/complexes of compounds useful for inhibiting the ADAM-IO protein and methods of making and purifying them are provided. Further provided are compositions comprising magnesium salts/complexes of the compounds in combination with a pharmaceutically acceptable carrier. The compounds well as such compositions comprising them are useful for the treatment of cancer, arthritis, diseases related to angiogenesis, such as renal diseases, heart diseases, such as heart failure, atherosclerosis, and stroke, inflammation, ulcer, infertility, scleroderma, endometriosis, mesothelioma, and diabetes. In addition, methods of treating forms of cancer, arthritis, and diseases related to angiogenesis in which ADAM-10 plays a critical role are provided.

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